510(k) K233597 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
Sonosite LX Ultrasound System
| Applicant | FUJIFILM Sonosite, Inc., Bothell WA, US |
| Decision | Substantially Equivalent, Dec 6, 2023 |
| Received | Nov 8, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233597
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.